The FDA says an electrical problem with recalled Philips' HeartStart ... about 700,000 defibrillators sold between 2005 and 2012. The recalled HeartStart FRx and HS1 (OnSite and Home) devices ...

The Philips HeartStart OnSite Defibrillator is designed to be the easiest-to-use, and most reliable defibrillator available. Available without a prescription from ActiveForever.com, the Philips ...

The FDA first approved home models of Philips AED devices in 2004. The defibrillators ... 2012 under the names HeartStart FRx, HeartStart HS1 Home, and HeartStart HS1 OnSite.

Philips’ HeartStart OnSite and HeartStart Home defibrillators are the only over-the-counter automated external defibrillators (AEDs) available to consumers in the US, while the HeartStart Home ...

Hundreds of thousands of automated external defibrillators (AEDs ... 2005 and 2012 under the names HeartStart FRx, HeartStart Home and HeartStart OnSite. About 700,000 of the devices were recalled ...

Business Leader Therapeutic Care at Philips. “This complements the premarket approval that we received last year for our HeartStart OnSite and HeartStart Home AEDs. Our industry leading ...

The therapy delivered by the HeartStart FR2+ is the most proven in the industry. More than 40 studies confirm its effectiveness. Philips’ high-current/low energy therapy ensures a potent ...

SILVER SPRING, Md. — The Food and Drug Administration on Tuesday issued a safety communication on HeartStart automated external defibrillators from Philips Healthcare, noting that certain ...

The Philips HeartStart OnSite Defibrillator is lightweight and easy to use. Providers can use the product to help save the lives of co-workers or residents, the firm notes.

In 2019, Philips received PMA approval for its HeartStart OnSite and HeartStart Home defibrillators, which are the only over-the-counter AEDs available to consumers in the U.S. [1] Model 861388 ...